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Article

Hypoplastic hippocampus in atypical Rett syndrome with a novel FOXG1 mutation.

Brain & development - 1 Jan 2018

Harada Kotoha, Yamamoto Mayumi, Konishi Yukihiko, Koyano Kaori, Takahashi Satoru, Namba Masanori, Kusaka Takashi

Abstract excerpt

The forkhead box G1 (FOXG1) gene encodes a brain-specific transcription factor and is associated with a congenital variant of atypical Rett syndrome (RTT); several FOXG1 mutations have been identified. The congenital variant of RTT shows a hypoplastic corpus callosum, delayed myelination, and frontal and temporal atrophy. Although no report has described a hippocampal abnormality in humans, the current study...

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Source

Identifiers

PMID: 28781028
DOI: 10.1016/j.braindev.2017.07.007

Genes

FOXG1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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